The present disclosure provides a rigid self-supporting MXene separation membrane and a preparation method and use thereof, belonging to the technical field of membranes. In the present disclosure, a MXene material is mixed with an aluminum salt powder to conduct one-step membrane formation by hot-pressing. The pressure forms the powder into a membrane and imparts rigidity, enabling a self-supporting structure; the heating breaks an ionic bond of an inorganic metal salt to reach a molten ionic state, and free metal cations react with active oxygen-containing functional groups on the surface of the MXene to form new chemical bonds (such as an Al—O bond); such a chemical bond has higher energy, achieving a desirable anti-swelling effect to improve the membrane stability. The separation membrane further has excellent conductivity and hydrophilicity.

An electrodeionization device having an improved boron rejection capability compared with high-performance electrodeionization devices proposed in the related art is provided. An electrodeionization device comprising a cathode; an anode; and a plurality of cation-exchange membranes and a plurality of anion-exchange membranes, the plurality of cation-exchange membranes and the plurality of anion-exchange membranes being arranged between the cathode and the anode so as to form concentrating compartments and desalting compartments, the concentrating compartments and desalting compartments being arranged alternately, the desalting compartments being filled with an ion-exchange resin, wherein the ion-exchange resin has an average particle size of 100 to 300 μm. Preferably, the ion-exchange resin has a uniformity coefficient of 1.1 or less.

Disclosed is a method of purifying a solution containing hydrofluoric acid, nitric acid and at least one silicon impurity by treating the solution with at least one reverse osmosis membrane. According to the method of the present invention, silicon impurities contained in the solution containing hydrofluoric acid and nitric acid can be selectively removed or reduced. This method can be advantageously used in the photovoltaic industry or in the battery component industry.

A water treatment assembly comprising a spiral wound hyperfiltration membrane module connected to: i) a feed line adapted for connection to a source of pressurized feed water, ii) a permeate line adapted for connection to a dispenser of treated water and iii) a concentrate line adapted for connection with drain; wherein the assembly further includes a pressurizable reservoir with valves for selectively diverting flow of pressurized feed water along the feed line, through the reservoir and returning to the feed line prior to passing through the hyperfiltration membrane module.

To provide a filter medium, a process for producing filter medium, a filtration device, a method for operating the filtration device, and a filtration system, which are capable of promptly regenerating the adsorption power by backwashing and realizing efficient operation of a filtration device. The filter medium of the present invention contains a carbon-based material in which a cumulative pore volume of pores having a pore radius of 2 nm or less is 25% or less with respect to a cumulative pore volume of pores having a pore radius of 50 nm or less.

A water purification system includes: a composite filter cartridge including a pretreatment filter cartridge and a filter membrane assembly; a raw water inlet pipe; a pure water outlet pipe; a pretreated water pipe; a booster pump; a water quality detecting device disposed to the raw water inlet pipe and/or the pure water outlet pipe and configured to detect water quality in the raw water inlet pipe and the pure water outlet pipe; and a control device connected to the water quality detecting device and configured to determine service life of the composite filter cartridge and/or judge whether the composite filter cartridge has lost efficacy according to information detected by the water quality detecting device.

Systems and processes for purifying and concentrating a liquid feed stream are disclosed. In the systems, the concentrated liquid output from the high pressure side of a reverse osmosis stage is used as the draw solution in the low pressure side of the reverse osmosis stage in a configuration called osmotically assisted reverse osmosis. This reduces the osmotic pressure differential across the membrane, permitting high solute concentrations to be obtained, hastening the purification of the liquid. Reduced system pressures are also obtained by arranging multiple osmotically assisted reverse osmosis stages in a cross-current arrangement. Overall system energy consumption is reduced compared to conventional thermal processes for high concentration streams.

Embodiments described herein relate to methods and systems for dewatering alcoholic solutions via forward osmosis.

This specification describes membrane based filtration and softening systems and methods. A system has a microfiltration or ultrafiltration (MF/UF) membrane unit upstream of a nanofiltration or reverse osmosis (NF/RO) membrane unit, optionally with no intermediate tank. In some cases, the system and method may be used with feed water provided at municipal line pressure to the membranes. NF/RO permeate is collected in a tank and then pumped to a header. Treated water may be drawn from the header for use or recycled to the system, for example to backwash or flush one or both of the membrane units. In a combined process, NF/RO permeate flushes the feed side of the NF/RO unit and then backwashes the MF/UF unit. In another process, the MF/UF unit and NF/RO unit are filled with NF/RO permeate before being placed in a standby mode.

The invention relates to methods for the synthesis of a thin-film composite membrane, comprising the following steps: a) providing an ultrafiltration porous support membrane, coated at the outer surface with a thin film, synthesized through interfacial polymerisation or interfacial initiation of polymerisation, b) contacting the membrane with a first solution comprising a first monomer, and allowing the solution to impregnate inside the thin film of the membrane, c) discarding the first solution comprising the first monomer, d) contacting the membrane with a second solution comprising a second monomer, and allowing the solution to impregnate inside the thin film of membrane, whereby the second monomer reacts with the first monomer and optionally with reactive groups of the thin film, e) discarding the second solution comprising the second monomer.